Primary malignant fibrous histiocytoma of the small bowel: a report of an additional case in duodenum.

Ze-sheng Wang, Cheng-long Xiong, Na Zhan, Guo-sheng Xiong, Hui Li, Hong Hu
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引用次数: 5

Abstract

Aims: We report herein an additional case of primary malignant fibrous histiocytoma (MFH) in the duodenum and provide a review of the existing literature.

Methods and results: A 61-yr-old Chinese man was admitted to our hospital with symptoms of melena, anorexia, and weight loss. An abdominal computed tomography (CT) and gastrointestinal barium meal examination demonstrated a tumor of the duodenum suggestive of primary malignancy. The tumor was successfully treated by pancreaticoduodenectomy. It was histopathologically and immunohistochemically diagnosed to be a storiform-type primary MFH of the duodenum. There have been a total of 40 cases of primary malignant fibrous histiocytoma of the small bowel documented in the literature including our Chinese cases.

Conclusion: Primary malignant fibrous histiocytoma of the small bowel, especially in the duodenum is extremely rare. The final diagnosis is made only after pathological and immunopathological examination of the tumor. The malignant potential of such tumors is high. The prognosis may be mainly dependent on the invasion and metastasis of tumor, while tumor size is irrelevant. The treatment should be surgery if possible. Early surgical intervention may be the best form of management that may offer the patient good result.

小肠原发性恶性纤维组织细胞瘤:附十二指肠一例报告。
目的:我们在此报告一例十二指肠原发性恶性纤维组织细胞瘤(MFH),并对现有文献进行复习。方法与结果:1例61岁中国男性以黑黑、厌食、体重下降等症状入院。腹部计算机断层扫描(CT)和胃肠道钡餐检查显示十二指肠肿瘤提示原发性恶性肿瘤。经胰十二指肠切除术成功治疗肿瘤。经组织病理学和免疫组织化学诊断为十二指肠的故事型原发性MFH。据文献报道,包括我们中国病例在内,共有40例原发性小肠恶性纤维组织细胞瘤。结论:原发性小肠恶性纤维组织细胞瘤,尤其是十二指肠恶性纤维组织细胞瘤极为罕见。最终的诊断只有在肿瘤的病理和免疫病理检查后才能做出。这种肿瘤的恶性可能性很高。预后可能主要取决于肿瘤的侵袭和转移,而与肿瘤大小无关。如果可能的话,治疗方法应该是手术。早期手术干预可能是最好的管理形式,可以为患者提供良好的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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